Canonical Allele Identifier: CA1728472248
Gene: LMTK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187236_98187237delinsAG , CM000669.2:g.98187236_98187237delinsAG GRCh38
NC_000007.13:g.97816548_97816549delinsAG , CM000669.1:g.97816548_97816549delinsAG GRCh37
NC_000007.12:g.97654484_97654485delinsAG NCBI36
NG_013375.1:g.85352_85353delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+238_998+239delinsAG MANE Select ENSP00000297293.5:n.998+238_998+239delinsAG
ENST00000297293.5:c.998+238_998+239delinsAG ENSP00000297293.5:n.998+238_998+239delinsAG
NM_014916.3:c.998+238_998+239delinsAG NP_055731.2:n.998+238_998+239delinsAG
XM_011515981.1:c.992+238_992+239delinsAG XP_011514283.1:n.992+238_992+239delinsAG
XM_011515981.3:c.992+238_992+239delinsAG XP_011514283.1:n.992+238_992+239delinsAG
NM_014916.4:c.998+238_998+239delinsAG MANE Select NP_055731.2:n.998+238_998+239delinsAG